About ClinCore
ClinCore plans, establishes and runs clinical trials at trial sites. We assist sponsors and investigators in achieving the goals of the study. ClinCore is committed to meeting the highest standards of quality while maintaining the safety and welfare of the trial participants. By adhering meticulously to GCP guidelines, regulatory requirements and ethical standards we enhance the trial’s reliability. ClinCore is a Bioforum Professional company – the professional services arm of Bioforum Applied Knowledge Center.
Recruitment:
- Targeted outreach to identified suitable candidates
- Active involvement in the ICF process – comprehensive explanation and preparation sessions before signing ICF/ICD
- Ensuring satisfactory recruitment rates and meeting study targets
- Accurate reporting: adhering to protocol requirements
- Skilled professional staffing services: allocation of trained and reliable coordinators
- Preparation for regulatory inspections and sponsors’ audit
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Our services encompass the entire lifecycle of the clinical trial:
- Coordinating the trial activities onsite
- Planning and establishing clinical trial units to meet study goals and regulatory requirements with maximum effectiveness:
- Implementation of quality systems according to ICH-GCP
- Development and implementation of internal SOPs
- Preparation of worksheets, questionnaires, study-specific forms and tracking tools
- Submission of pack preparation, obtaining approvals from ethics committees and regulatory authorities
- Training of study staff and the parties involved in the trial: laboratory staff, pharmacists, dietitians and more.
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